Allele Registry

Canonical Allele Identifier: PA104677

Gene: OCRL HGNC NCBI

ClinVar Allele:

25898

ClinVar RCV:

RCV000011606

ClinVar Variation:

10859

HGVS (amino-acid)	Matching Registered Transcripts
NP_000267.2:p.His524Gln	CA255585 NM_000276.4:c.1572C>G CA414616529 NM_000276.4:c.1572C>A